Fan M Z, Stoll B, Jiang R, Burrin D G
USDA, ARS, Children's Nutrition Research Center, Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA.
J Anim Sci. 2001 Feb;79(2):371-81. doi: 10.2527/2001.792371x.
Our objective was to examine the distribution of enterocyte digestive enzyme activity along the crypt-villus and longitudinal axes of the small intestine in formula-fed neonatal pigs between the ages of 14 and 18 d. The distended intestinal sac method was used to isolate 12 sequential fractions (F1 through F12) of epithelial cells. Enterocyte migration rate was measured in the proximal and distal intestine using in vivo bromodeoxyuridine labeling. Specific activities of representative villus cell marker enzymes of alkaline phosphatase, aminopeptidase N, sucrase, and lactase increased 6- to 17-fold from F12 (crypt cells) to F1 (villus cells), whereas the crypt cell marker [3H]thymidine incorporation increased 8- to 18-fold from F1 (villus cells) to F12 (crypt cells). Enterocyte migration rate was similar (3.2 vs 3.0 microm/h), whereas the villus height (547.4 vs 908.5 microm) and enterocyte life span (4.7 vs 10.2 d) were markedly lower (P < 0.05) in the proximal than in the distal segments, respectively. In general, the specific activities of all enzymes were lowest in the crypt fractions (F9 through F12) but increased markedly (ranging from 8- to 17-fold) from F12 to F1. The activity of aminopeptidase N was higher and that of sucrase was lower in the distal than in the proximal segment. The activities of the remaining enzymes were similar in the proximal and the distal segments. Our results suggest that the enterocyte life span in the distal small intestine is approximately twice as long as in the proximal small intestine. However, despite the difference in life span, the patterns of enzyme activities along the crypt-villus axis were generally similar in the proximal and the distal regions.
我们的目的是研究14至18日龄配方奶喂养新生仔猪小肠隐窝-绒毛轴和纵轴上肠上皮细胞消化酶活性的分布。采用扩张肠囊法分离上皮细胞的12个连续部分(F1至F12)。使用体内溴脱氧尿苷标记法测量近端和远端小肠中的肠上皮细胞迁移率。碱性磷酸酶、氨肽酶N、蔗糖酶和乳糖酶等代表性绒毛细胞标记酶的比活性从F12(隐窝细胞)到F1(绒毛细胞)增加了6至17倍,而隐窝细胞标记物[3H]胸苷掺入量从F1(绒毛细胞)到F12(隐窝细胞)增加了8至18倍。肠上皮细胞迁移率相似(3.2对3.0微米/小时),而近端段的绒毛高度(分别为547.4对908.5微米)和肠上皮细胞寿命(4.7对10.2天)明显低于远端段(P<0.05)。一般来说,所有酶的比活性在隐窝部分(F9至F12)最低,但从F12到F1显著增加(8至17倍)。远端段氨肽酶N的活性较高,蔗糖酶的活性较低。其余酶在近端和远端段的活性相似。我们的结果表明,远端小肠中的肠上皮细胞寿命约为近端小肠的两倍。然而,尽管寿命存在差异,但近端和远端区域沿隐窝-绒毛轴的酶活性模式通常相似。